SG11202005926XA - SALT OF PYRAZOLO[1,5-a]PYRIMIDINE COMPOUND AND CRYSTALS THEREOF - Google Patents

SALT OF PYRAZOLO[1,5-a]PYRIMIDINE COMPOUND AND CRYSTALS THEREOF

Info

Publication number
SG11202005926XA
SG11202005926XA SG11202005926XA SG11202005926XA SG11202005926XA SG 11202005926X A SG11202005926X A SG 11202005926XA SG 11202005926X A SG11202005926X A SG 11202005926XA SG 11202005926X A SG11202005926X A SG 11202005926XA SG 11202005926X A SG11202005926X A SG 11202005926XA
Authority
SG
Singapore
Prior art keywords
pyrazolo
crystals
salt
pyrimidine compound
pyrimidine
Prior art date
Application number
SG11202005926XA
Other languages
English (en)
Inventor
Taro Yamashita
Original Assignee
Eisai R&D Man Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Eisai R&D Man Co Ltd filed Critical Eisai R&D Man Co Ltd
Publication of SG11202005926XA publication Critical patent/SG11202005926XA/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Dermatology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
SG11202005926XA 2018-02-26 2019-02-22 SALT OF PYRAZOLO[1,5-a]PYRIMIDINE COMPOUND AND CRYSTALS THEREOF SG11202005926XA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2018031646 2018-02-26
PCT/JP2019/006850 WO2019163956A1 (fr) 2018-02-26 2019-02-22 SEL DE COMPOSÉ PYRAZOLO [1,5-a] PYRIMIDINE ET CRISTAUX DE CELUI-CI

Publications (1)

Publication Number Publication Date
SG11202005926XA true SG11202005926XA (en) 2020-07-29

Family

ID=67687243

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11202005926XA SG11202005926XA (en) 2018-02-26 2019-02-22 SALT OF PYRAZOLO[1,5-a]PYRIMIDINE COMPOUND AND CRYSTALS THEREOF

Country Status (14)

Country Link
US (1) US11312720B2 (fr)
EP (1) EP3760631B1 (fr)
JP (1) JP7257376B2 (fr)
KR (1) KR20200124655A (fr)
CN (1) CN111655694B (fr)
AU (1) AU2019224410A1 (fr)
BR (1) BR112020015729A2 (fr)
CA (1) CA3088718A1 (fr)
IL (1) IL276160A (fr)
MX (1) MX2020008110A (fr)
RU (1) RU2020125450A (fr)
SG (1) SG11202005926XA (fr)
TW (1) TW201936607A (fr)
WO (1) WO2019163956A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11141418B1 (en) * 2018-06-22 2021-10-12 The Board Of Regents, The University Of Texas System Methods and compositions for KRAS inhibitors
WO2021106864A1 (fr) * 2019-11-25 2021-06-03 Eisai R&D Management Co., Ltd. Procédé de préparation de dérivés de pyrazolo [1,5-a] pyrimidine
CA3220630A1 (fr) 2021-06-02 2022-12-08 Otsuka Pharmaceutical Co., Ltd. Compose pyrazolo[1,5-a]pyrimidine pour le traitement de troubles dermiques
WO2023233033A1 (fr) 2022-06-03 2023-12-07 Domain Therapeutics Nouveaux inhibiteurs de par-2

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1506196B1 (fr) 2001-11-01 2012-01-18 Icagen, Inc. Pyrazolopyrimidines en tant que bloqueurs du canal sodium
JP2003286171A (ja) * 2002-03-28 2003-10-07 Sumitomo Pharmaceut Co Ltd Par阻害剤
JP2004170323A (ja) 2002-11-22 2004-06-17 Sumitomo Pharmaceut Co Ltd 皮膚疾患治療剤のスクリーニング方法
WO2005030773A1 (fr) 2003-09-26 2005-04-07 Dainippon Sumitomo Pharma Co., Ltd. Nouveaux derives pyrazolopyrimidine
ES2540867T3 (es) 2010-02-26 2015-07-14 Mitsubishi Tanabe Pharma Corporation Compuestos de pirazolopirimidina y su uso como inhibidores de PDE10
WO2012080735A1 (fr) 2010-12-16 2012-06-21 Convergence Pharmaceuticals Limited Dérivés pyrrolopyrimidine inhibant ask1
GB201101517D0 (en) 2011-01-28 2011-03-16 Proximagen Ltd Receptor antagonists
JP5531066B2 (ja) 2011-08-24 2014-06-25 田辺三菱製薬株式会社 ピラゾロピリミジン化合物及びpde10阻害剤としてのその使用
WO2015048245A1 (fr) * 2013-09-25 2015-04-02 Vertex Pharmaceuticals Incorporated Imidazopyridazines utiles en tant qu'inhibiteurs de la voie de signalisation par-2
WO2018043461A1 (fr) 2016-08-31 2018-03-08 エーザイ・アール・アンド・ディー・マネジメント株式会社 COMPOSÉ DE PYRAZOLO [1,5-a] PYRIMIDINE

Also Published As

Publication number Publication date
BR112020015729A2 (pt) 2020-12-08
US20210107907A1 (en) 2021-04-15
CN111655694B (zh) 2023-03-28
KR20200124655A (ko) 2020-11-03
EP3760631A1 (fr) 2021-01-06
IL276160A (en) 2020-09-30
JPWO2019163956A1 (ja) 2021-02-04
US11312720B2 (en) 2022-04-26
WO2019163956A1 (fr) 2019-08-29
CN111655694A (zh) 2020-09-11
RU2020125450A3 (fr) 2022-03-28
EP3760631A4 (fr) 2021-10-20
JP7257376B2 (ja) 2023-04-13
RU2020125450A (ru) 2022-03-28
EP3760631B1 (fr) 2023-11-08
MX2020008110A (es) 2020-11-06
TW201936607A (zh) 2019-09-16
CA3088718A1 (fr) 2019-08-29
AU2019224410A1 (en) 2020-07-09

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